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Biomarkers for primary biliary cholangitis: current perspectives

Primary biliary cholangitis (PBC) is a chronic progressive cholestatic disease characterized by destruction of small- and medium-sized intrahepatic bile ducts. It is no longer a rare disease, since many new asymptomatic cases are incidentally identified. Liver biopsy is diagnostically critical but n...

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Autores principales: Kouroumalis, Elias, Samonakis, Demetrius, Voumvouraki, Argyro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014437/
https://www.ncbi.nlm.nih.gov/pubmed/29950909
http://dx.doi.org/10.2147/HMER.S135337
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author Kouroumalis, Elias
Samonakis, Demetrius
Voumvouraki, Argyro
author_facet Kouroumalis, Elias
Samonakis, Demetrius
Voumvouraki, Argyro
author_sort Kouroumalis, Elias
collection PubMed
description Primary biliary cholangitis (PBC) is a chronic progressive cholestatic disease characterized by destruction of small- and medium-sized intrahepatic bile ducts. It is no longer a rare disease, since many new asymptomatic cases are incidentally identified. Liver biopsy is diagnostically critical but not always feasible or practical to be performed. Many potential, noninvasive, markers have been proposed to replace liver biopsy and further provide the assessment of disease severity and ultimate prognosis. In this review, we evaluated serum biomarkers proposed for diagnosis, extent of fibrosis, disease prognosis and attempts for early prediction of treatment response. Older biochemical and immunological markers are presented along with recent reports including the role of microRNAs and promising results based on proteomics and metabolomics.
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spelling pubmed-60144372018-06-27 Biomarkers for primary biliary cholangitis: current perspectives Kouroumalis, Elias Samonakis, Demetrius Voumvouraki, Argyro Hepat Med Review Primary biliary cholangitis (PBC) is a chronic progressive cholestatic disease characterized by destruction of small- and medium-sized intrahepatic bile ducts. It is no longer a rare disease, since many new asymptomatic cases are incidentally identified. Liver biopsy is diagnostically critical but not always feasible or practical to be performed. Many potential, noninvasive, markers have been proposed to replace liver biopsy and further provide the assessment of disease severity and ultimate prognosis. In this review, we evaluated serum biomarkers proposed for diagnosis, extent of fibrosis, disease prognosis and attempts for early prediction of treatment response. Older biochemical and immunological markers are presented along with recent reports including the role of microRNAs and promising results based on proteomics and metabolomics. Dove Medical Press 2018-06-18 /pmc/articles/PMC6014437/ /pubmed/29950909 http://dx.doi.org/10.2147/HMER.S135337 Text en © 2018 Kouroumalis et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Kouroumalis, Elias
Samonakis, Demetrius
Voumvouraki, Argyro
Biomarkers for primary biliary cholangitis: current perspectives
title Biomarkers for primary biliary cholangitis: current perspectives
title_full Biomarkers for primary biliary cholangitis: current perspectives
title_fullStr Biomarkers for primary biliary cholangitis: current perspectives
title_full_unstemmed Biomarkers for primary biliary cholangitis: current perspectives
title_short Biomarkers for primary biliary cholangitis: current perspectives
title_sort biomarkers for primary biliary cholangitis: current perspectives
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6014437/
https://www.ncbi.nlm.nih.gov/pubmed/29950909
http://dx.doi.org/10.2147/HMER.S135337
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